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1. Schembl16586788
2. Al01211
3. Al-01211
4. N-[(1r,2r)-2-(3-chloro-4-cyclopropoxyphenyl)-2-hydroxy-1-(pyrrolidinylmethyl)ethyl]-2-(6-chloro(2-naphthyl))-2-(hydroxyimino)acetamide
| Molecular Weight | 542.4 g/mol |
|---|---|
| Molecular Formula | C28H29Cl2N3O4 |
| XLogP3 | 6.4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 9 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 94.4 |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 806 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of AL01211 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right AL01211 manufacturer or AL01211 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred AL01211 manufacturer or AL01211 supplier.
PharmaCompass also assists you with knowing the AL01211 API Price utilized in the formulation of products. AL01211 API Price is not always fixed or binding as the AL01211 Price is obtained through a variety of data sources. The AL01211 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AL01211 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AL01211, including repackagers and relabelers. The FDA regulates AL01211 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AL01211 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A AL01211 supplier is an individual or a company that provides AL01211 active pharmaceutical ingredient (API) or AL01211 finished formulations upon request. The AL01211 suppliers may include AL01211 API manufacturers, exporters, distributors and traders.
AL01211 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of AL01211 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right AL01211 GMP manufacturer or AL01211 GMP API supplier for your needs.
A AL01211 CoA (Certificate of Analysis) is a formal document that attests to AL01211's compliance with AL01211 specifications and serves as a tool for batch-level quality control.
AL01211 CoA mostly includes findings from lab analyses of a specific batch. For each AL01211 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
AL01211 may be tested according to a variety of international standards, such as European Pharmacopoeia (AL01211 EP), AL01211 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AL01211 USP).
